Asymmetric reduction of prochiral aromatic ketones by Borane-Amine complexes in the presence of a chiral amine-BF < inf > 3 < /inf > catalyst

dc.contributor.author Kanth, J. V.Bhaskar
dc.contributor.author Periasamy, Mariappan
dc.date.accessioned 2022-03-27T09:12:29Z
dc.date.available 2022-03-27T09:12:29Z
dc.date.issued 1990-12-01
dc.description.abstract The (-)-N-α-Methylbenzyl-3,5-dihydrodinaphthazepine-BH3 complex reduces aromatic ketones to alcohols with 11-57% enantiomeric excess (e.e.) in the presence of BF3·OEt2, the (-)-N-α-methylbenzyl-3,5 dihydrodinaphthazepine-BF3 complex catalyses asymmetric reduction of acetophenone by N,N′-diethylaniline- BH3 to give α-phenylethyl alcohol in 51% e.e.
dc.identifier.citation Journal of the Chemical Society, Chemical Communications
dc.identifier.issn 00224936
dc.identifier.uri 10.1039/C39900001145
dc.identifier.uri http://xlink.rsc.org/?DOI=C39900001145
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12585
dc.title Asymmetric reduction of prochiral aromatic ketones by Borane-Amine complexes in the presence of a chiral amine-BF < inf > 3 < /inf > catalyst
dc.type Journal. Article
dspace.entity.type
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